2-(6-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethyl-2-oxoacetamide → 2-(6-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine

HRID 1404082Notes

Reaction equation

HRID 1404082 reaction equation
[CH2:1]([O:8][C:9]1[C:17]([F:18])=[CH:16][CH:15]=[C:14]2[C:10]=1[C:11]([CH2:19][CH2:20][N:21]([CH3:23])[CH3:22])=[CH:12][NH:13]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1C=C2C(C(C(=O)C(N(C)C)=O)=CN2)=CC=1F)C1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[CH:10]=[C:14]2[C:15]([C:11]([CH2:19][CH2:20][N:21]([CH3:22])[CH3:23])=[CH:12][NH:13]2)=[CH:16][C:17]=1[F:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 583039052-(6-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethyl-2-oxoacetamideHCID 669270882-(4-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine

Product 1

HCID 583040102-(6-Benzyloxy-5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamineYield 77%

Procedure

Following the procedure used to prepare compound 1-7a (step 6 scheme 1), compound 4-4 gave compound 4-5 in 77% yield as a brown oil.

Sources & evidence

ORD record
ord-981be939268c483ba62729f73be9a499
Source dataset
uspto-grants-2014_12
Patent number
US08912220B2

Reaction notes

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